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NCT06027749 · ClinicalTrials.gov registry record · NA

Impact of Capturing Ictal Events With Ultra-long-term Ambulatory EEG Monitoring With Remote EEG Monitoring System.

A NA study of Epilepsy and Seizures, sponsored by Epitel.

Recruiting
Registry status
NA
Development phase
65
Enrollment target
2
Study locations

NCT06027749 is a NA study of Epilepsy and Seizures that is actively recruiting participants, run by Epitel. The registered enrollment target is 65 participants, below the 952-participant average among 160 other Epilepsy trials with a reported enrollment target (93% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT06027749, a NA study of Epilepsy and Seizures, is actively recruiting participants, sponsored by Epitel.

RECRUITING
Registry status
NA
Development phase
65 participants
Enrollment target
2
Study locations

Study Summary

The goal of this clinical trial is to test Epitel's™ Remote EEG Monitoring System's (REMI™) ability to record electroencephalography (EEG) of seizure events in an ambulatory setting for extended periods (14 - 28 days) in patients presenting with questionable seizure characterization. The main questions it aims to answer are: • Can more seizure events be recorded in fourteen (14) days than can be recorded in three (3) days? • Do treating clinicians find clinical value in extended fourteen (14) - twenty-eight (28) days of EEG? Participants will wear a portable EEG device (REMI) for fourteen (14) to twenty-eight (28) days in their home/community setting.

Conditions Studied

Interventions

  • DEVICE Epitel's™ Remote EEG Monitoring System's (REMI™)

Study Locations (2)

Florida

  • University of South Florida - Tampa

South Carolina

  • Medical University of South Carolina - Charleston

Trial Details

FieldValue
Enrollment Target 65 participants
Start Date 2023-10-13
Est. Completion 2025-06-01
Phase NA

Sponsor

Epitel

1 total trials

What the Registry Record Tells You About NCT06027749

The ClinicalTrials.gov registry entry for NCT06027749 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 65 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 952-participant average among 160 other Epilepsy trials with a reported enrollment target (93% lower). The listed sponsor is Epitel, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Epilepsy appearing as the primary indexed condition, and to 1 intervention - of which Epitel's™ Remote EEG Monitoring System's (REMI™) is the first listed.

NCT06027749 reports 2 study locations spanning 2 distinct geographic areas - top geographies include Florida, South Carolina.

Frequently Asked Questions

What is clinical trial NCT06027749 about?

NCT06027749 is a clinical study titled "Impact of Capturing Ictal Events With Ultra-long-term Ambulatory EEG Monitoring With Remote EEG Monitoring System.". The goal of this clinical trial is to test Epitel's™ Remote EEG Monitoring System's (REMI™) ability to record electroencephalography (EEG) of seizure events in an ambulatory setting for extended periods (14 - 28 days) in patients presenting with questionable seizure characterization. The main questi...

What is the current status of trial NCT06027749?

This trial is currently recruiting. It is a NA study. The enrollment target is 65 participants. The study started on 2023-10-13. Estimated completion is 2025-06-01.

What conditions does trial NCT06027749 study?

This clinical trial studies the following conditions: Epilepsy, Seizures.

What interventions are being tested in trial NCT06027749?

The interventions under investigation include: Epitel's™ Remote EEG Monitoring System's (REMI™) (DEVICE).

Who is sponsoring clinical trial NCT06027749?

This trial is sponsored by Epitel, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06027749 being conducted?

This trial has 2 study locations across Florida, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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